Hagemans M L C, Winkel L P F, Van Doorn P A, Hop W J C, Loonen M C B, Reuser A J J, Van der Ploeg A T
Department of Metabolic Diseases and Genetics, Erasmus MC-Sophia, Rotterdam, The Netherlands.
Brain. 2005 Mar;128(Pt 3):671-7. doi: 10.1093/brain/awh384. Epub 2005 Jan 19.
Late-onset Pompe's disease (acid maltase deficiency, glycogen storage disease type II) is a slowly progressive myopathy caused by deficiency of acid alpha-glucosidase. Current developments in enzyme replacement therapy require detailed knowledge of the kind and severity of symptoms and the natural course of the disease in the patient population. A detailed questionnaire covering the patients' medical history and current situation was developed and information was gathered from 54 Dutch patients. The mean age of the participants was 48.6 +/- 15.6 years. The first complaints started at a mean age of 28.1 +/- 14.3 years and were mostly related to mobility problems and limb-girdle weakness. Fifty-eight percent of the adult patients indicated the presence of mild muscular symptoms during childhood. Twenty-eight percent of the patients waited >5 years for the final diagnosis after the first visit to a physician for disease-related complaints. At the time of questionnaire completion, 48% of the study population used a wheelchair and 37% used artificial ventilation. Movements such as rising from an armchair, taking stairs or getting upright after bending over were difficult or impossible for more than two-thirds of the respondents. The age at onset, the rate of disease progression and the sequence of respiratory and skeletal muscle involvement varied substantially between patients. Seventy-six percent of the participants indicated being troubled by fatigue and 46% by pain. This survey has mapped the age at onset, presenting symptoms, heterogeneity in progression and range of disease severity in a large group of Dutch patients. We conclude that early manifestations in childhood require proper attention to prevent unnecessary delay of the diagnosis. The follow-up of patients with late-onset Pompe's disease should focus on respiratory and limb-girdle muscle function, the capacity to perform daily activities, and the presentation of fatigue and pain.
晚发型庞贝病(酸性麦芽糖酶缺乏症,糖原贮积病II型)是一种由酸性α-葡萄糖苷酶缺乏引起的缓慢进展性肌病。酶替代疗法的当前进展需要详细了解患者群体中症状的类型和严重程度以及疾病的自然病程。我们制定了一份涵盖患者病史和当前状况的详细问卷,并从54名荷兰患者那里收集了信息。参与者的平均年龄为48.6±15.6岁。最初的症状开始于平均28.1±14.3岁,主要与活动问题和肢带肌无力有关。58%的成年患者表示在儿童期存在轻度肌肉症状。28%的患者在因与疾病相关的症状首次就诊后等待超过5年才得到最终诊断。在完成问卷时,48%的研究人群使用轮椅,37%使用人工通气。对于超过三分之二的受访者来说,从扶手椅起身、上楼梯或弯腰后起身等动作困难或无法完成。患者之间的发病年龄、疾病进展速度以及呼吸和骨骼肌受累的顺序差异很大。76%的参与者表示受疲劳困扰,46%受疼痛困扰。这项调查描绘了一大群荷兰患者的发病年龄、呈现的症状、进展的异质性和疾病严重程度范围。我们得出结论,儿童期的早期表现需要得到适当关注,以防止诊断的不必要延迟。晚发型庞贝病患者的随访应关注呼吸和肢带肌功能、进行日常活动的能力以及疲劳和疼痛的表现。